eSense Skin Response
EC Declaration of Conformity
according to the following guidelines:
2014/30/EU OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 26 February 2014
on harmonizing the laws of the Member States relating to electromagnetic compatibility.
RoHS substance bans (2011/65/EU)
WEEE Waste Electrical and Electronic Equipment (2002/96/EC & 2008/34/EC)
The manufacturer / Distributor / Authorized representative
Mindfield Biosystems Ltd.
WEEE-Reg.-Nr. DE 24465971
hereby declares that the following product:
“Mindfield® eSense Muscle”
follows the provisions of the guidelines identified above and their amendments in force at the time of the declaration.
The following harmonized standards have been applied:
DIN EN 62368-1:2016-05 Equipment for audio and video, information and communication technology – Part 1: Safety requirements
DIN EN 61326-1; VDE 0843-20-1:2013-07 Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 1: General requirements (IEC 61326-1:2012); German version EN 61326-1:2013
DIN EN 61326-2-2; VDE 0843-20-2-2:2013-08 Electrical equipment for measurement, control, and laboratory use – EMC requirements – Part 2: Electrical equipment for measurement, control, and laboratory use Part 2-2: Particular requirements – Test arrangement, operating conditions and performance characteristics for the portable test, measurement and monitoring equipment for use in low-voltage power supply systems (IEC 61326-2-2:2012); German version EN 61326-2-2:2013
Date: 05. May 2021
Niko Rockensüß, Managing Director